Neurodevelopmental disorders such as autism spectrum disorder (ASD) and psychiatric disorders, for example, schizophrenia (SCZ) represent a large spectrum of disorders that manifest through cognitive and behavioural problems. ASD and SCZ are both highly heritable, and some phenotypic similarities between ASD and SCZ have sparked an interest in understanding their genetic commonalities. The genetics of both disorders exhibit significant heterogeneity. Developments in genomics and systems biology, continually increases people’s understanding of these disorders. Recently, pathogenic genetic variants in the regulatory factor X (RFX) family of transcription factors have been identified in a number of ASD cases. In this thesis, common genetic variants and expression patterns of genes identified to have a conserved promotor X-Box motif region, a binding site of RFX factors, are studied. Significant common variants identified through expression quantitative trait loci (eQTLs) and genome wide association studies (GWAS) are mapped to the regulatory regions of these genes and analysed for putative enrichment. In addition, single-cell RNA sequencing data is utilised to examine enrichment of cell types having high X-Box gene expression in the developing human cortex. Through the study, genes that have eQTLs or SNPs in the genomic regulatory regions of the X-Box genes have been identified. While there were no eQTLs or GWAS SNPs in the X-Box motifs, in the X-Box promoter regions some common variants were found. By hypergeometric distribution testing and the subsequent p-values obtained, all of these distributions are statistically under-enriched. Further, major cell types in the cortical region with increased expression of the X-Box genes and most expressed genes among these enriched cell types have been identified. Among the 11 cell types seven were found to be enriched for X-Box genes and many of the most expressed genes in these cell-types were similar. A further study into the cell types and genes identified, along with additional systems biological data analysis, could reveal a larger list of X-Box genes involved in ASD and SCZ and the specific roles of these genes.
Identifer | oai:union.ndltd.org:UPSALLA1/oai:DiVA.org:uu-445493 |
Date | January 2021 |
Creators | Ganesan, Abhishekapriya |
Publisher | Uppsala universitet, Institutionen för biologisk grundutbildning |
Source Sets | DiVA Archive at Upsalla University |
Language | English |
Detected Language | English |
Type | Student thesis, info:eu-repo/semantics/bachelorThesis, text |
Format | application/pdf |
Rights | info:eu-repo/semantics/openAccess |
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